RS12770228 Unknown gene

Other Chr 10:21494705
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What This Variant Does
"rs12770228 is a SNP in a region on ch 10p12.31 designated as the chromosome 10 open reading frame 11..."
GWAS Studies (6)
Trait Risk Allele OR / Beta P-value Study
Severe, life-threatening illness (confirmatory factor analysis Factor 20) 3E-14 PubMed
Whole body fat mass (UKB data field 23100) A β: 0.018 3E-12 PubMed
Smoking initiation (ever regular vs never regular) A β: 0.016 8E-11 PubMed
Body mass index G β: 0.018 6E-9 PubMed
Superior parietal thickness β: 0.039 2E-8 PubMed
Parental longevity (mother's age at death) A β: 0.013 5E-6 PubMed
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